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Achromobacter xylosoxidans isolates exhibit genome diversity, variable virulence, high levels of antibiotic resistance, and potential intrahost evolution
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Abstract
Achromobacter xylosoxidans is an emerging pathogen characterized by high levels of antibiotic resistance (AR) and increasing infection rates worldwide. This motile, opportunistic pathogen is widely distributed in the environment and can cause various infections, including pneumonia, bacteremia, endocarditis, meningitis, and others. In this study, we analyzed the population structure, AR profiles, and virulence factors of over 200 publicly available genomes. Core genome analysis revealed that A. xylosoxidans is highly adaptable, possessing a relatively small core genome. Antibiotic susceptibility testing of isolates from the United States revealed high resistance to multiple antibiotics. Our data show that imipenem/relebactam is as effective against A. xylosoxidans as imipenem alone, indicating that relebactam does not inhibit β-lactamase activity in Achromobacter . The species features multiple secretion systems, including the Type III secretion system of the YscN family, which is similar to those found in Bordetella pertussis and Pseudomonas aeruginosa . Isolates collected from the same patients showed changes in cytotoxicity, flagella motility, biofilm, and AR, suggesting their dynamic adaptation to the host environment. Intra-host evolved isolates, NIH-010, NIH-016, and NIH-018, demonstrated the loss of flagellar motility and variable cytotoxicity while exhibiting increased AR and enhanced biofilm formation. Sequence analysis suggests that NIH-016-3 has a tyrosine to histidine mutation at position 330 near the FlhF guanosine triphosphate-binding domain that may affect flagellar assembly. Interestingly, virulence assays showed significant variation in the ability of different A. xylosoxidans isolates to induce cell death in in vitro models, suggesting their dynamic adaptation to the host environment. IMPORTANCE: This study provides a comprehensive examination of Achromobacter xylosoxidans , an emerging pathogen of global concern due to its high antibiotic resistance (AR) and increasing clinical relevance. By analyzing over 200 genomes, we offer critical insights into the population structure, resistance mechanisms, and virulence factors of this species. The identification of a small core genome underscores its potential for genomic plasticity. The existence of multiple secretion systems highlights the great capacity of A. xylosoxidans as a pathogen. Variations in virulence among A. xylosoxidans isolates indicate the complexity of this pathogen, underscoring the need for further studies on its virulence mechanisms. Evolution within the host includes the loss of motility-associated systems and enhanced AR and biofilm formation. This work showed that A. xylosoxidans is resistant to relebactam when combined with imipenem, a combination effective in other bacteria. These findings emphasize the urgent need for targeted therapeutic strategies to combat this opportunistic pathogen.
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Metadata
- Authors
- Acharya, P., Lloyd, C., Lam, N. T., Kumke, J., Ray, S., Yanira Muñoz Ramirez, Z., Das, S., & Lam, H. N.
- Affiliations
- Virginia Tech (US)
- Ton Duc Thang University (VN)
- National Institutes of Health (US)
- Facultad de Ciencias Químicas, Universidad Autónoma de Chihuahua
- Corresponding author
- Lam, Hanh Ngoc
- Venue
- mSphere
- Publisher
- American Society for Microbiology
- Published
- 2026-02-24
- Volume
- 11
- Issue
- 2
- Pages
- e0087025-e0087025
- ISSN
- 2379-5042 (ISSN-L)
- PMC
- PMC12931269
- OpenAlex
- W7127336502
- Cited by
- 8
- References
- 111
- Citations by year
- 2026: 8
- FWCI
- 35.17
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- cc-by
- journals.asm.org/non-commercial-tdm-license (tdm)
- Locations
- mSphere (publishedVersion, cc-by)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion)
- PubMed (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed Central (submittedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- National Institute of Allergy and Infectious Diseases (R00AI139281)
- Division of Intramural Research (1ZIACL090107)
- Topics
- Health Sciences › Medicine › Microbiology (medical) › Infections and bacterial resistance
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bacterial biofilms and quorum sensing
- Health Sciences › Medicine › Microbiology (medical) › Antibiotic Resistance in Bacteria
- Keywords
- antibiotic resistance, virulence factors, population structure, core genome, flagellar motility, biofilm formation, cytotoxicity, type III secretion system, imipenem resistance, relebactam, secretion systems, genome plasticity, host adaptation, clinical isolates
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
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Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.